240136-69-0 Usage
Uses
Used in Pharmaceutical Industry:
2-AMINO-4-(3-NITROPHENYL)PYRIMIDINE is used as a pharmaceutical agent for its anti-inflammatory and anti-cancer properties. Its biological activities make it a promising candidate for the development of new drugs to treat various inflammatory and cancerous conditions.
Used in Agrochemical Industry:
2-AMINO-4-(3-NITROPHENYL)PYRIMIDINE is used as an agrochemical agent, leveraging its biological activities to control or prevent pests and diseases in agriculture.
Used as an Intermediate in Organic Synthesis:
2-AMINO-4-(3-NITROPHENYL)PYRIMIDINE serves as an intermediate in the synthesis of various organic compounds, contributing to the development of new chemical entities with diverse applications.
Used in Chemical Modification:
The nitrophenyl group in 2-AMINO-4-(3-NITROPHENYL)PYRIMIDINE allows for easy functionalization, making it an attractive target for chemical modification. This enables the development of new compounds with enhanced properties and expanded applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 240136-69-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,0,1,3 and 6 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 240136-69:
(8*2)+(7*4)+(6*0)+(5*1)+(4*3)+(3*6)+(2*6)+(1*9)=100
100 % 10 = 0
So 240136-69-0 is a valid CAS Registry Number.
240136-69-0Relevant academic research and scientific papers
4 - Phenyl - 2 - amino pyrimidine compound and its preparation method and application
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Paragraph 0054-0055, (2018/03/24)
The invention discloses a 4-phenyl-2-aminopyrimidine compound, the structure of which is shown in the general formula I, wherein X is shown in the specification, R0 is hydrogen, methyl or ethyl; R1 is hydrogen, methyl, ethyl or isopropyl; R2 is isopropyl,
Assessment of new triplet forming artificial nucleobases as RNA ligands directed towards HCV IRES IIId loop
Safir Filho, Mauro,Martin, Anthony R.,Benhida, Rachid
, p. 1780 - 1783 (2017/04/03)
We report the synthesis of two new artificial nucleobase scaffolds, 1 and 2, featuring adequate hydrogen bonding donors and acceptors for the molecular recognition of U:A and C:G base pairs, respectively. The tethering of these structures to various amino acids and the assessment of these artificial nucleobase-amino acid conjugates as RNA ligands against a model of HCV IRES IIId domain are also reported. Compound 1e displayed the highest affinity (Kd twice lower than neomycin – control). Moreover, it appears that this interaction is enthalpically and entropically favored.
